Extended knowledge of N-Boc-2-Amino-5-bromopyridine

With the rapid development of chemical substances, we look forward to future research findings about 159451-66-8.

As we all know, there are many different methods for the synthesis of a compound, and people can choose the synthesis method that suits their own laboratory according to the actual situation. 159451-66-8, name is N-Boc-2-Amino-5-bromopyridine, molecular formula is C10H13BrN2O2, The compound is widely used in many fields, so it is necessary to find a new synthetic route. The downstream synthesis method of this compound is introduced below. Computed Properties of C10H13BrN2O2

To a solution of 1B (7.65 g, 28 mmol) in THF (50 mL)-MeOH (50 mL) at RT was added phenylboronic acid (6.83 g, 56 mmol), PXPd (500 mg, 0.93 mmol), followed by K2CO3 (15.5 g, 112 mmol). The reaction mixture was stirred at 70 C. in a preheated oil bath for 1 h. After this time, the reaction mixture was cooled to RT. The reaction mixture was poured into water (100 mL), and the resultant mixture was extracted with EtOAc (3¡Á100 mL). The combined organic layers were washed with saturated NaCl. The organic layer was dried (Na2SO4), filtered and concentrated. The resulting residue was purified by silica gel (120 g) column chromatography eluting with a gradient of EtOAc (0-60%) in hexane to give the title compound as an off-white solid (5.4 g, 72%). LC/MS (method A): retention time=3.07 min, (M+H)+=271.

With the rapid development of chemical substances, we look forward to future research findings about 159451-66-8.

Reference:
Patent; Sun, Chongqing; Ewing, William R.; Sulsky, Richard B.; Huang, Yanting; US2006/155126; (2006); A1;,
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem